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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2000033890 |
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最近更新日期: Date of Last Refreshed on: |
2020-06-15 16:54:26 |
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注册时间: Date of Registration: |
2020-06-15 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
清达颗粒治疗高血压(1级、低中危)患者的临床疗效评价---多中心、随机、双盲双模拟、平行对照的非劣效临床研究 |
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Public title: |
Clinical efficacy evaluation of Qingda Granule in the treatment of hypertension (grade 1, low to medium-risk) patients: a multicenter, randomized, double-blind, double-simulated, parallel-controlled, non-inferiority clinical study |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
清达颗粒治疗高血压(1级、低中危)患者的临床疗效评价---多中心、随机、双盲双模拟、平行对照的非劣效临床研究 |
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Scientific title: |
Clinical efficacy evaluation of Qingda Granule in the treatment of hypertension (grade 1, low to medium-risk) patients: a multicenter, randomized, double-blind, double-simulated, parallel-controlled, non-inferiority clinical study |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
ChiMCTR2000003400 |
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申请注册联系人: |
陈盛君 |
研究负责人: |
付长庚 |
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Applicant: |
Shengjun Chen |
Study leader: |
Changgeng Fu |
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申请注册联系人电话: Applicant telephone: |
+86 15370230291 |
研究负责人电话: Study leader's telephone: |
+86 15101038490 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
chensj@tianjiang.com |
研究负责人电子邮件: Study leader's E-mail: |
fucgbs@163.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
江苏省江阴市高新区新胜路1号 |
研究负责人通讯地址: |
北京市海淀区西苑操场1号 |
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Applicant address: |
1 Xinsheng Road, High-Tech Zone, Jiangyin, Jiangsu, China |
Study leader's address: |
1 Xiyuan Playground, Haidian District, Beijing, China |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
江阴天江药业有限公司 |
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Applicant's institution: |
Jiangyin Tianjiang Pharmaceutical Co. LTD. |
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研究负责人所在单位: |
中国中医科学院西苑医院 |
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Affiliation of the Leader: |
Xiyuan Hospital, China Academy of Chinese Medical Sciences |
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是否获伦理委员会批准: |
是/Yes |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
中国中医科学院西苑医院医学伦理委员会2020XLA027-3 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
中国中医科学院西苑医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Xiyuan Hospital, China Academy of Chinese Medical Sciences |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-05-31 00:00:00 |
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伦理委员会联系人: |
訾明杰 |
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Contact Name of the ethic committee: |
Mingjie Zi |
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伦理委员会联系地址: |
北京市海淀区西苑操场1号 |
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Contact Address of the ethic committee: |
1 Xiyuan Playground, Haidian District, Beijing, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
中国中医科学院西苑医院 |
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Primary sponsor: |
Xiyuan Hospital, Chinese Academy of Chinese Medical Sciences |
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研究实施负责(组长)单位地址: |
北京市海淀区西苑操场1号 |
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Primary sponsor's address: |
1 Xiyuan Playground, Haidian District, Beijing, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
申办方 |
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Source(s) of funding: |
The management |
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Target disease: |
hypertension |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
评价清达颗粒治疗高血压(1级、低中危)患者的有效性及安全性。 |
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Objectives of Study: |
To evaluate the efficacy and safety of Qingda granule in the treatment of patients with hypertension (grade 1, low risk). |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
1.符合统一诊室血压测量的原发性高血压病诊断标准,高血压分级为1级、危险分层属低中危者(参照《中国高血压防治指南》2018年修订版); |
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Inclusion criteria |
1. Meet the diagnostic criteria for essential hypertension measured in the same clinic, the hypertension is graded as grade 1, and the risk stratification is low to medium risk (refer to the 2018 Revision of Chinese Guidelines for The Prevention and Treatment of Hypertension); |
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排除标准: |
1.患有明显肝肾疾患或ALT、AST高于ULN1.5倍,Cr、BUN高于ULN; |
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Exclusion criteria: |
1. Patients with obvious liver and kidney diseases or with ALT and AST 1.5 times higher than ULN, Cr and BUN higher than ULN; |
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研究实施时间: Study execute time: |
从 From 2020-06-01 00:00:00至 To 2021-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2020-06-01 00:00:00 至 To 2021-06-30 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
采用分层、区组随机方法,以中心为分层因素,在各中心内进行区组随机化,随机表由不参与本试验统计分析的统计师使用SAS统计软件按分层因素和分组比例产生。区组个数、区组长度、随机初值种子参数等作为保密数据与随机表一起密封在不透光的文件袋中,作为一级盲底。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Stratification and district-group randomization were adopted, with the center as the stratification factor, and district-group randomization was carried out in each center. The random table was generated by statisticians not involved in the statistical analysis of this experiment using SAS statistical software. |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
双盲 |
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Blinding: |
Double blind |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
No |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
申办方 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
sponsor |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |